Piebaldism is a rare autosomal dominant disorder of melanocyte development.: Common characteristics include a congenital white forelock, scattered. Abstract. AVINA FIERRO, Jorge Arturo and HERNANDEZ AVINA, Daniel Alejandro. Piebaldism, partial albinism in the hair and the skin. Rev Cubana Pediatr. Piebaldismo, import ancia de su seguimient o zyxwvutsrqponm Robert o Glor¡ o\ o Carbia^, Alberto Solari^ y Alberto W oscof f RES UMEN: El piebaldism o es.
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Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. These mutations do not allow the correct development of the melanoblast and the posterior migration from the neural crest to a definitive site.
Piebaldismo, importancia de su seguimiento | Roberto Glorio –
This page was last edited on 14 Mayat All who inherit the gene have at some time in life evidence of piebald hypopigmentation of the hair or skin, most likely both. Incontinentia pigmenti Scratch dermatitis Shiitake mushroom dermatitis. Additional information Further information on this disease Classification s 2 Gene s 2 Clinical signs and symptoms Publications in PubMed Other website s 3.
Rebecca Heckard, la modella affetta da piebaldismo
To learn more about the cookies we use, check out our Cookies policy. For security reasons we are asking you to please enter your Toluna password to access the site. Albinism Oculocutaneous albinism Ocular albinism. For all other comments, please send your remarks via contact us. These mutations result in a decrease of the receptor tyrosine kinase signalling.
Type I cytokine receptor: Seminars in Cutaneous Medicine and Surgery. Oculocutaneous albinism Ocular albinism. Specialised Social Services Eurordis directory.
Views Read Edit View history. In albinism the cells lack the ability to produce pigment altogether. From Wikipedia, the free encyclopedia. Piebaldism is a kind of neurocristopathyinvolving defects of various neural crest cell lineages that include melanocytes, but also involving many other tissues derived from the neural crest. Infobox medical condition All articles with unsourced statements Articles with unsourced statements from October Articles to be expanded from April All articles to be expanded Articles using small message boxes.
InfancyNeonatal ICD Piebaldism This condition affects melanocyte development Classification and external resources Specialty endocrinology [ edit on Wikidata ].
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We’re working on it PTH1R Jansen’s metaphyseal chondrodysplasia. Skin color Skin whitening Tanning Sunless.
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Retrieved from ” https: What do you think? Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli—Franceschetti—Jadassohn syndrome Dyskeratosis congenita Piebaldism reticulate pigmentary disorder Galli—Galli disease Revesz syndrome. Your Facebook token has expired, you need to reconnect your Toluna account with Facebook or disconnect the two accounts for now.
Like in the offline world, cookies make things better. Proceedings of the National Academy of Sciences. Sign Up Sign in. This section needs expansion. Users should refer to the original published version of the material for the full abstract. Log in to Toluna or.
In other projects Wikimedia Commons. Piebaldism is a rare autosomal dominant disorder of melanocyte development. Disease definition Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas leukoderma on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock poliosisand in some cases piebaldiamo hypopigmented and depigmented eyebrows and eyelashes.
Share your opinions with the world. Vasospastic macule Woronoff’s ring Nevus anemicus. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Amino acid metabolism disorders Autosomal dominant disorders Disturbances of human pigmentation Disturbances of pigmentation. CASR Familial hypocalciuric hypercalcemia.